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The emerging roles of CDK12 in tumorigenesis

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00027162%3A_____%2F17%3AN0000130" target="_blank" >RIV/00027162:_____/17:N0000130 - isvavai.cz</a>

  • Result on the web

    <a href="https://celldiv.biomedcentral.com/articles/10.1186/s13008-017-0033-x" target="_blank" >https://celldiv.biomedcentral.com/articles/10.1186/s13008-017-0033-x</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1186/s13008-017-0033-x" target="_blank" >10.1186/s13008-017-0033-x</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    The emerging roles of CDK12 in tumorigenesis

  • Original language description

    Cyclin-dependent kinases (CDKs) are key regulators of both cell cycle progression and transcription. Since dysregulation of CDKs is a frequently occurring event driving tumorigenesis, CDKs have been tested extensively as targets for cancer therapy. Cyclin-dependent kinase 12 (CDK12) is a transcription-associated kinase which participates in various cellular processes, including DNA damage response, development and cellular differentiation, as well as splicing and pre-mRNA processing. CDK12 mutations and amplification have been recently reported in different types of malignancies, including loss-of-function mutations in high-grade serous ovarian carcinomas, and that has led to assumption that CDK12 is a tumor suppressor. On the contrary, CDK12 overexpression in other tumors suggests the possibility that CDK12 has oncogenic properties, similarly to other transcription-associated kinases. In this review, we discuss current knowledge concerning the role of CDK12 in ovarian and breast tumorigenesis and the potential for chemical inhibitors of CDK12 in future cancer treatment.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10608 - Biochemistry and molecular biology

Result continuities

  • Project

    <a href="/en/project/NV16-34152A" target="_blank" >NV16-34152A: Targeting ovarian tumors to experimental drugs by inhibition of CDK12 kinase activity</a><br>

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2017

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Cell Division

  • ISSN

    1747-1028

  • e-ISSN

  • Volume of the periodical

  • Issue of the periodical within the volume

    12

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    10

  • Pages from-to

    7

  • UT code for WoS article

    000414013700001

  • EID of the result in the Scopus database